1. Published Data Registry
  2. View publication

View publication

↩ Back to all publications
Publication
PropertyValue
Working Groups Winkelmann
SubprojectNone
Open AccessNo
Publication TypeLetter
Peer ReviewedYes
PMIDPubMed ID 36202297
DOIDOI 10.1016/j.ejmg.2022.104635
Publication Year2022
TitleA de novo BCL11B variant case manifesting with dystonic movement disorder regarding the article "BCL11B-related disorder in two canadian children: Expanding the clinical phenotype (Prasad et al., 2020).". Wikidata
JournalEuropean journal of medical genetics
ISSN1769-7212
ESSN1878-0849
URL https://www.ncbi.nlm.nih.gov/pubmed/?term=36202297%5Buid%5D
Pages104635
Issue11
Volume65
Journal AbbreviationEur J Med Genet
AuthorsHarrer P, Leppmeier V, Berger A, Demund S, Winkelmann J, Berweck S, Zech M
First AuthorHarrer P
Last AuthorZech M
ScholiaScholia Wikidata-based representation at Scholia

 External Resources

 Q115215126  Wikidata ID